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Τι (ποιος) είναι X-linked lymphoproliferative disease - ορισμός
X-linked lymphoproliferative disease
LYMPHOPROLIFERATIVE DISORDER
Duncan's disease; X-linked lymphoproliferative syndrome; Purtilo syndrome; XLP (hematology)
X-linked lymphoproliferative disease (also known as Duncan disease or Purtilo syndrome and abbreviated as XLP) is a lymphoproliferative disorder, usually caused by SH2DIA gene mutations in males. XLP-positive individuals experience immune system deficiencies that render them unable to effectively respond to the Epstein-Barr virus (EBV), a common virus in humans that typically induces mild symptoms or infectious mononucleosis (IM) in patients.
Lymphoproliferative disorders
PRIMARY IMMUNODEFICIENCY DISEASE CHARACTERIZED BY IMMUNE DYSREGULATION TYPICALLY AFTER VIRAL INFECTION, USUALLY ASSOCIATED WITH EPSTEIN-BARR VIRAL INFECTION
Lymphoproliferative; Lymphoproliferative disorder; Immunoproliferative diseases; Lymphoproliferative disease; Lymphoproliferative diseases; B-cell lymphoproliferative disease
Lymphoproliferative disorders (LPDs) refer to a specific class of diagnoses, comprising a group of several conditions, in which lymphocytes are produced in excessive quantities. These disorders primarily present in patients who have a compromised immune system.
X-linked dominant inheritance
MODE OF INHERITANCE
X-linked dominance; X-linked dominant
X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type.
